ghd
- 网络生长激素缺乏症
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Meanwhile , ghd iron , support for3D effects in films and games is also growing source .
与此同时,生长激素缺乏症铁,三维电影和游戏效果支持也越来越大来源。
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Research on Separating and Robustness GHD Signal in Wireless Channel
广义双曲线分布信号在无线信道中分离和鲁棒性的研究
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GHD is an international professional services company .
GHD是一家国际化设计谘询公司。
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Cheap Ghd she had told me the whole truth .
但是我不敢肯定她是否已告诉了我全部实情。
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Conclusion IGF-1 and leptin regulate growth in children with GHD in their individual way .
结论IGF1和瘦素对GHD患儿生长发育的调节作用是相互独立的。
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Furthermore 21.3 % of idiopathic GHD were also complicated with apparent central hypothyroidism .
21.3%的特发性GHD合并中枢性甲状腺功能减退。
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To evaluate changes in cardiac structure and function in GHD patients treated with recombinant human growth hormone ( r-hGH ) .
目的评价用人重组生长激素(r-hGH)治疗原发性生长激素缺乏症患者时心脏结构和功能变化。
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Conclusion The use of China-made r-hGH to treat the children with GHD is effective and safe .
结论国产r-hGH治疗儿童GHD安全,有效。
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In general , confirmation of the diagnosis of adult GHD in both groups usually requires an appropriate growth hormone stimulation test .
一般来说,对于两组中的成人GHD的诊断确认通常需要采用一种适宜的生长激素刺激试验。
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In patients with GHD , central ( secondary ) hypothyroidism may first become evident or worsen during somatropin treatment .
患有GHD的患者,在采用生长激素治疗时,中央(次级)肾上腺机能衰退会首次变得明显或恶化。
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Project supported by the Presidential Foundation of the Chinese Academy of Sciences , hair ghd , China ( Grant No. ) .
中国科学院院长基金(批准号:)资助的课题。
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The detection of IGF 1 and IGFBP 3 will be helpful for the correct diagnosis of GHD ;
2检测血清IGF-1和IGFBP-3将有助于儿童GHD的正确诊断;
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Method Serum IGF-1 and leptin levels were measured by immunoradiometric assay in 20 prepuberal normal children and 23 children with GHD .
方法用放射免疫法分别检测20例正常青春期前儿童和23例GHD患儿血清IGF1和瘦素的水平。
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GHD has outstanding opportunities for professionals to apply and develop their skills across a broad range of industries , and within a culturally diverse international company .
GHD作为一家以多元文化为特色的国际性大公司,为各种专业人员在各个领域间运用和发展各自的业务技能提供优良的机会。
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Results The serum levels of IGF-1 and IGFBP-3 were significantly lower in GHD than those in non-GH deficient short stature and control group .
非GH缺乏性矮身材组患儿血清IGF-1和IGFBP-3水平低于正常对照组(P<0.01),高于GHD组患儿,差别有统计学意义(P<0.05)。
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There was no difference in FAHSDS between children with isolated GHD and those with multiple hormone deficiencies ( P > 0.05 ) .
孤立性GHD患儿的FAHSDS与由垂体病变引起的多激素缺乏症患儿相比差异无统计学意义(P>0.05)。
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The sensitivity of IGF-1 in GHD was 100 % , the specificity was 80 % , the accuracy of test was 77.5 % .
GHD组IGF-1敏感性为100%,特异性80%,试验正确性77.5%;
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Context : The effects of GH replacement in GH-deficient ( GHD ) adults previously treated for acromegaly are not well known .
内容:在原先肢端肥大症治愈继发生长激素缺乏的患者中使用生长激素替代治疗的影响尚不明确。
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Conclusion Determination of serum IGF-1 and IGFBP-3 levels could be applied for screening and diagnosis of GHD , even possibly replacing the classic GH provocative test .
结论:IGF-1和IGFBP-3的检测可能可作为筛查和诊断GHD有价值的指标,血清IGF-1、IGFBP-3水平的检测可能可替代GH激发试验。
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The sensitivity of IGFBP-3 in GHD was 77.5 % , the specificity was 62.5 % , the accuracy of test was 65 % .
IGFBP-3的敏感性为77.5%,特异性62.5%,试验正确性65%;
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Objective Growth hormone deficiency ( GHD ) is the important cause of short stature in children and GH-replacement therapy has been recommended for treatment of GHD .
目的生长激素缺乏症(growthhormonedeficiency,GHD)是导致儿童身材矮小的重要原因。
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Objective To study the relationship between the clinical manifestations and changes of pituitary magnetic resonance imaging ( MRI ) in short stature children with growth hormone deficiency ( GHD ) .
目的研究生长激素缺乏(GHD)矮小儿童临床表现与垂体MRI之间的关系。
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Methods : Nine children with GHD were given China-made r-hGH of 0 . 1IU / kg . d for 6 months .
方法:选择GHD患儿9例,给予国产r-hGH0.1IU/kg·d,疗程6个月。
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Oral glucose tolerance test ( OGTT ) and insulin releasing test ( IRT ) were also performed 3 months before and after the therapy in 15 children with GHD .
对其中15例在治疗前及治疗后3个月进行口服葡萄糖耐量试验(OGTT)和胰岛素(INS)释放试验(IRT)。
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The sensitivity of IGF-1 and IGFBP-3 measured simultaneously in GHD were 77.5 % , the specificity were 60 % , the accuracy of test were 62.5 % .
IGF-1和IGFBP-3同时检测,其敏感性为77.5%,特异性60%,试验正确性62.5%。
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Objective To evaluate the diagnostic value of biochemical tests ( GH stimulation tests , IGF - ⅰ and IGFBP-3 ) in short children suspected with growth hormone deficiency ( GHD ) .
目的以临床诊断作为矮小症患儿(可疑GHD)诊断标准,评估生长激素激发试验、胰岛素样生长因子Ⅰ(IGFⅠ)及IGF结合蛋白3(IGFBP3)对GHD的诊断价值。
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Methods One and two dimensional echocardiography was applied in 9 patients with primary GHD pre and after treatment with r-hGH , compared with another 20 normal adolescents matched in age and sex as control group .
方法对9例确诊为原发性生长激素缺乏患者用r-hGH治疗前后及对20例年龄、性别相匹配的正常青少年通过一维和二维心超检查。
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Serum IGFBP 3 protease activity in GHD increased to ( 29.0 ± 6.8 ) % after treatment with recombining human somatropin ( rhGH ) for six months .
用重组人GH(rhGH)治疗6个月后,GHD患者的血清IGFBP3蛋白酶活性上升至(29.0±6.8)%。
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Blood samples of 20 boys with growth hormone deficiency ( GHD ) and 10 boys with idiopathic short stature ( ISS ) were collected at various time points during different hGH provocative tests .
对30例矮小男童(20例GH缺乏症和10例特发性矮小症)在不同的激发试验各时间点采血,以放射免疫法测定血浆胃促生长素水平。
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The results showed that the serun leptin levels were ( 1.22 ± 0.94 ) ng / ml in prepuberal normal children and ( 3.079 ± 2.407 ) ng / ml in GHD children before treatment .
结果显示,正常青春期前儿童血清leptin水平为(1.22±0.94)ng/ml;